Fasting serum bile acids concentration is associated with insulin resistance independently of diabetes status

胰岛素抵抗 内科学 医学 2型糖尿病 平衡 糖尿病 肥胖 内分泌学 2型糖尿病 队列 空腹血糖受损 胰岛素 葡萄糖稳态 糖耐量受损
作者
Sang‐Guk Lee,Yong‐ho Lee,Eunhye Choi,Yonggeun Cho,Jeong‐Ho Kim
出处
期刊:Clinical Chemistry and Laboratory Medicine [De Gruyter]
卷期号:57 (8): 1218-1228 被引量:28
标识
DOI:10.1515/cclm-2018-0741
摘要

Abstract Background Bile acids (BAs) have been demonstrated to exert a variety of metabolic effects and alterations in BAs have been reported in patients with obesity, insulin resistance (IR) and type 2 diabetes mellitus (T2DM). However, it is unclear which metabolic condition is the main contributor to alterations in BAs. In this study, we investigate the associations between different BA profiles with glycemia, obesity or IR status. Methods Fasting serum concentrations of 15 BA species were determined in a total of 241 individuals (71 drug-naïve patients with T2DM, 95 patients with impaired fasting glucose [IFG], and 75 healthy controls. Results A comparison of the mean values of the BAs revealed no significant differences between normoglycemic controls and patients with IFG or T2DM. However, when the entire cohort was divided according to the presence of IR as determined by a homeostasis model assessment of insulin resistance (HOMA-IR) value >2.5, the levels of total BA and most species of BAs were significantly higher in patients with IR than in patients without. In the correlation analysis, most species of BAs, as well as total BA, were significantly associated with HOMA-IR levels. Furthermore, when the subjects were divided into four groups according to IR and diabetic status, subjects with IR had significantly higher total BAs than participants without IR both in diabetic and non-diabetic groups. Ultimately, multiple linear regression analysis identified HOMA-IR as the only significant contributor to most serum BA species. Conclusions Our findings support the essential role of IR in regulating BA metabolism and that this effect is independent of diabetic status.
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